Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9470361 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 12
rs883079
TBX5
1.000 0.080 12 114355435 3 prime UTR variant C/G;T snv 1.8E-05; 0.61 3
rs9912468
PRKCA
17 66322239 intron variant G/A;C snv 3
rs2242285
SLC25A26 ; LRIG1
3 66381178 intron variant A/C;G snv 2
rs7342028
VTI1A
10 112719503 intron variant G/C;T snv 2
rs1344852 4 20182314 intergenic variant G/A;C;T snv 1
rs1562782
CAND1.11 ; AMPD3
11 10321164 intron variant A/C;G snv 1
rs2207790
NFIA
1 61432295 intron variant G/A;T snv 1
rs7198919
LITAF
16 11595035 intron variant T/A;C snv 1
rs7211246
NSRP1
17 30158744 intron variant A/G;T snv 1
rs17391905 1 51080468 intergenic variant T/G snv 3.7E-02 2
rs7771320 6 7502516 upstream gene variant T/C snv 5.4E-02 1
rs6683273
PRDM16
1 3342619 intron variant A/G snv 6.8E-02 1
rs11700980
N6AMT1
21 28781917 regulatory region variant T/C snv 8.7E-02 1
rs13195040
ZNF184
1.000 0.040 6 27446145 downstream gene variant A/G snv 9.0E-02 2
rs17608766
LRRC37A2 ; GOSR2
1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 8
rs11708996
SCN5A
0.925 0.120 3 38592432 intron variant G/C snv 0.11 6
rs1419856 7 35267372 intergenic variant A/G snv 0.11 1
rs1362212 7 35265695 intergenic variant G/A snv 0.11 2
rs359466
CPEB4
5 173888863 5 prime UTR variant C/G snv 0.11 1
rs12764182
LRMDA
10 76131488 intron variant T/G snv 0.16 1
rs11710077
SCN5A
3 38616408 intron variant A/T snv 0.17 3
rs7537765
CLCN6
1 11827246 intron variant A/G snv 0.15 0.18 1
rs3770770
STRN
2 36965723 intron variant C/T snv 0.18 1
rs17020136
HEATR5B
2 37020872 intron variant T/C snv 0.24 0.18 2